A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15961912



Internal ID19687166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53512278..53707229hg38UCSC Ensembl
chr19:54015532..54210483hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38194952
hg19194952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4255561
Supporting Variants
Samples
Known GenesDPRX, LOC284379, MIR1283-1, MIR1323, MIR498, MIR512-1, MIR512-2, MIR515-1, MIR515-2, MIR518B, MIR518F, MIR519B, MIR519C, MIR519E, MIR520A, MIR520B, MIR520E, MIR520F, MIR523, MIR525, MIR526A1, MIR526B, ZNF331
MethodSequencing
AnalysisSV calls were generated using multi-algorithm consensus pipeline involving raw evidence assessment, filtering, clustering, genotyping, alternative allele structure resolution, and gene annotation. These methods are described in detail in the gnomAD-SV preprint [Collins*, Brand*, et al., bioRxiv (2019)|https://www.biorxiv.org/content/10.1101/578674v1], and are largely based on methods developed in [Werling et al., Nat. Genet. (2018)|https://www.ncbi.nlm.nih.gov/pubmed/29700473].
Platform
Comments
ReferencegnomAD_Structural_Variants
Pubmed ID12345678
Accession Number(s)nssv15961912
Frequency
Sample Size10847
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000138


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